Chromosome imbalances in syndromic hearing loss. (Record no. 19202792)

MARC details
000 -LEADER
fixed length control field 01423 a2200469 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515191010.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201002s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1399-0004
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1111/j.1399-0004.2009.01276.x
Source of number or code doi
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Catelani, A L P M
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20100225
245 00 - TITLE STATEMENT
Title Chromosome imbalances in syndromic hearing loss.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Clinical genetics
Date of publication, distribution, etc. Nov 2009
300 ## - PHYSICAL DESCRIPTION
Extent 458-64 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Child
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Child, Preschool
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosomal Instability
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Comparative Genomic Hybridization
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Female
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Gene Dosage
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hearing Loss
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Humans
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Male
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Syndrome
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Krepischi, A C V
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kim, C A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kok, F
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Otto, P A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Auricchio, M T B M
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mazzeu, J F
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Uehara, D T
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Costa, S S
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Knijnenburg, J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tabith, A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Vianna-Morgante, A M
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mingroni-Netto, R C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Rosenberg, C
773 0# - HOST ITEM ENTRY
Title Clinical genetics
Related parts vol. 76
-- no. 5
-- p. 458-64
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/j.1399-0004.2009.01276.x">https://doi.org/10.1111/j.1399-0004.2009.01276.x</a>
Public note Available from publisher's website

No items available.